Basic Genetics Flashcards

1
Q

What is heterochromatin?

A

Heterochromatin

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2
Q

Stains as light bands and consists of highly condensed regions that are usually not transcriptionally
active

A

Achromatin

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3
Q

Stains as light bands and consists of highly condensed regions that are usually not transcriptionally
active

A

Eurochromatin

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4
Q

Humans have a complement of 46 chromosomes arranged into23 pairs; one member of each pair is
inherited from the father and the other from the mother.Each of the members of one chromosome
pair is referred to as a autosomal homologue.

A

1st one correct: 2nd incorrect (chromosome)

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5
Q

Mitosis is the process of cell division unique to gametes (ova and sperm). In contrast to meiosis, the
process of mitosis produces four gametes with genetic variability. This results in four unique, rather
than two identical, daughter cells. Meiosis is the process of replication in nucleated body cells (except ova and sperm cells).

A

Both false. Interchanged.

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6
Q

During this period, the nucleolus (nucleoli) becomes visible, and the chromosomes are
extended and active metabolically. The cell synthesizes RNA and protein in preparation for
cell division.

A

G1 (Gap 1)

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7
Q

This is the time of DNA replication, during which both growth and metabolic activities are
minimal.
The centrosome is also duplicated during the S stage.

A

S phase (DNA synthesis)

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8
Q

Relatively short, lasting approximately 4 to 5 hours

A

G2 (Gap 2)

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9
Q

Last stage of interphase.

A

G2 (Gap 2)

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10
Q

Give the steps in the Mphase/ Mitosis phase in chronological order.

A

Prophase
Metaphase
Anaphase
Telophase
(PMAT)

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11
Q

Sister chromatids move to the equatorial plate

A

Metaphase

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12
Q

The chromatin becomes tightly coiled.
Nucleolus and nuclear envelope disintegrate.
Centrioles move to opposite poles of the cell

A

Prophase

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13
Q

A segment of DNA arranged along the chromosome at a specific position called locus

A

Gene

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14
Q

Total genetic composition of an individual, representing maternally and paternally derived genes. It is the
complement of DNA that is inherited.

A

Genotype

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15
Q

Normal number of human chromosomes?
Autosomes?

A

46 (1 pair of 23 chromosomes from each parent)
44 autosomes (1pair of 22 chromosomes from each parent)

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16
Q

State that genes for different traits are inherited separately from each other. This allows for all
possible combinations of genes to occur in the offspring

A

Law of Assortment

17
Q

Any change in the structure or sequence of DNA, whether it is physical or biochemical.

A

Mutation

18
Q

What is the simplest type of mutation, in which only one nucleotide in the DNA
sequence is changed?

A

Point mutation

19
Q

Results in a change in a codon, which alters the amino acid in the corresponding
peptide

A

Missense mutation

20
Q

results when a point change in one of the nucleotides of a DNA sequence causes one of the three possible stop codons to
be formed

A

Nonsense mutation

21
Q

Give rise to pseudogenes and other so-called junk DNA that does not code for proteins
E.g glycophorin A and B genes; the second involves the genes RHD and RHCE. The Chido and Rodgers
blood group antigens, carried on the complement components of the C4A and C4B genes.

A

Duplication

22
Q

An example of such an event resulting in a hybrid formation is seen in the MNSs blood group system.

A

Recombination

23
Q

initiation, elongation, and termination

A

Translation

24
Q

organelles composed of proteins and ribosomal RNA (rRNA)

A

Ribosomes